Differential Urinary Proteome Analysis for Predicting Prognosis in Type 2 Diabetes Patients with and without Renal Dysfunction
Renal dysfunction, a major complication of type 2 diabetes, can be predicted from estimated glomerular filtration rate (eGFR) and protein markers such as albumin concentration. Urinary protein biomarkers may be used to monitor or predict patient status. Urine samples were selected from patients enro...
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doaj-41b1dc6bec31436bbc0386c67b1611992020-11-25T03:38:25ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672020-06-01214236423610.3390/ijms21124236Differential Urinary Proteome Analysis for Predicting Prognosis in Type 2 Diabetes Patients with and without Renal DysfunctionHee-Sung Ahn0Jong Ho Kim1Hwangkyo Jeong2Jiyoung Yu3Jeonghun Yeom4Sang Heon Song5Sang Soo Kim6In Joo Kim7Kyunggon Kim8Asan Institute for Life Sciences, Asan Medical Center, Seoul 05505, KoreaDepartment of Internal Medicine, Pusan National University Hospital, Pusan 49241, KoreaDepartment of Biomedical Sciences, University of Ulsan College of Medicine, Seoul 05505, KoreaAsan Institute for Life Sciences, Asan Medical Center, Seoul 05505, KoreaConvergence Medicine Research Center, Asan Institute for Life Sciences, Seoul 05505, KoreaDepartment of Internal Medicine, Pusan National University Hospital, Pusan 49241, KoreaDepartment of Internal Medicine, Pusan National University Hospital, Pusan 49241, KoreaDepartment of Internal Medicine, Pusan National University Hospital, Pusan 49241, KoreaAsan Institute for Life Sciences, Asan Medical Center, Seoul 05505, KoreaRenal dysfunction, a major complication of type 2 diabetes, can be predicted from estimated glomerular filtration rate (eGFR) and protein markers such as albumin concentration. Urinary protein biomarkers may be used to monitor or predict patient status. Urine samples were selected from patients enrolled in the retrospective diabetic kidney disease (DKD) study, including 35 with good and 19 with poor prognosis. After removal of albumin and immunoglobulin, the remaining proteins were reduced, alkylated, digested, and analyzed qualitatively and quantitatively with a nano LC-MS platform. Each protein was identified, and its concentration normalized to that of creatinine. A prognostic model of DKD was formulated based on the adjusted quantities of each protein in the two groups. Of 1296 proteins identified in the 54 urine samples, 66 were differentially abundant in the two groups (area under the curve (AUC): <i>p</i>-value < 0.05), but none showed significantly better performance than albumin. To improve the predictive power by multivariate analysis, five proteins (ACP2, CTSA, GM2A, MUC1, and SPARCL1) were selected as significant by an AUC-based random forest method. The application of two classifiers—support vector machine and random forest—showed that the multivariate model performed better than univariate analysis of mucin-1 (AUC: 0.935 vs. 0.791) and albumin (AUC: 1.0 vs. 0.722). The urinary proteome can reflect kidney function directly and can predict the prognosis of patients with chronic kidney dysfunction. Classification based on five urinary proteins may better predict the prognosis of DKD patients than urinary albumin concentration or eGFR.https://www.mdpi.com/1422-0067/21/12/4236urinediabetic kidney diseasekidney functionproteomicsmass spectrometrystatistical clinical model |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Hee-Sung Ahn Jong Ho Kim Hwangkyo Jeong Jiyoung Yu Jeonghun Yeom Sang Heon Song Sang Soo Kim In Joo Kim Kyunggon Kim |
spellingShingle |
Hee-Sung Ahn Jong Ho Kim Hwangkyo Jeong Jiyoung Yu Jeonghun Yeom Sang Heon Song Sang Soo Kim In Joo Kim Kyunggon Kim Differential Urinary Proteome Analysis for Predicting Prognosis in Type 2 Diabetes Patients with and without Renal Dysfunction International Journal of Molecular Sciences urine diabetic kidney disease kidney function proteomics mass spectrometry statistical clinical model |
author_facet |
Hee-Sung Ahn Jong Ho Kim Hwangkyo Jeong Jiyoung Yu Jeonghun Yeom Sang Heon Song Sang Soo Kim In Joo Kim Kyunggon Kim |
author_sort |
Hee-Sung Ahn |
title |
Differential Urinary Proteome Analysis for Predicting Prognosis in Type 2 Diabetes Patients with and without Renal Dysfunction |
title_short |
Differential Urinary Proteome Analysis for Predicting Prognosis in Type 2 Diabetes Patients with and without Renal Dysfunction |
title_full |
Differential Urinary Proteome Analysis for Predicting Prognosis in Type 2 Diabetes Patients with and without Renal Dysfunction |
title_fullStr |
Differential Urinary Proteome Analysis for Predicting Prognosis in Type 2 Diabetes Patients with and without Renal Dysfunction |
title_full_unstemmed |
Differential Urinary Proteome Analysis for Predicting Prognosis in Type 2 Diabetes Patients with and without Renal Dysfunction |
title_sort |
differential urinary proteome analysis for predicting prognosis in type 2 diabetes patients with and without renal dysfunction |
publisher |
MDPI AG |
series |
International Journal of Molecular Sciences |
issn |
1661-6596 1422-0067 |
publishDate |
2020-06-01 |
description |
Renal dysfunction, a major complication of type 2 diabetes, can be predicted from estimated glomerular filtration rate (eGFR) and protein markers such as albumin concentration. Urinary protein biomarkers may be used to monitor or predict patient status. Urine samples were selected from patients enrolled in the retrospective diabetic kidney disease (DKD) study, including 35 with good and 19 with poor prognosis. After removal of albumin and immunoglobulin, the remaining proteins were reduced, alkylated, digested, and analyzed qualitatively and quantitatively with a nano LC-MS platform. Each protein was identified, and its concentration normalized to that of creatinine. A prognostic model of DKD was formulated based on the adjusted quantities of each protein in the two groups. Of 1296 proteins identified in the 54 urine samples, 66 were differentially abundant in the two groups (area under the curve (AUC): <i>p</i>-value < 0.05), but none showed significantly better performance than albumin. To improve the predictive power by multivariate analysis, five proteins (ACP2, CTSA, GM2A, MUC1, and SPARCL1) were selected as significant by an AUC-based random forest method. The application of two classifiers—support vector machine and random forest—showed that the multivariate model performed better than univariate analysis of mucin-1 (AUC: 0.935 vs. 0.791) and albumin (AUC: 1.0 vs. 0.722). The urinary proteome can reflect kidney function directly and can predict the prognosis of patients with chronic kidney dysfunction. Classification based on five urinary proteins may better predict the prognosis of DKD patients than urinary albumin concentration or eGFR. |
topic |
urine diabetic kidney disease kidney function proteomics mass spectrometry statistical clinical model |
url |
https://www.mdpi.com/1422-0067/21/12/4236 |
work_keys_str_mv |
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